ADGB

androglobin

Summary

Predicted to enable several functions, including calcium-dependent cysteine-type endopeptidase activity; heme binding activity; and oxygen binding activity. Predicted to be involved in spermatid development. Predicted to be located in sperm flagellum. Predicted to be active in sperm annulus and sperm midpiece. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants99 total

rsidPosition (GRCh37)AllelesClassClinVar
rs22756066:146,918,950G/Aupstream gene variant
rs24844160906:146,920,204G/Auncertain significance
rs7486265186:146,920,223C/Guncertain significance
rs11921255706:146,920,226C/Tuncertain significance
rs5623659996:146,956,563G/Auncertain significance
rs760714906:146,977,900T/Clikely benign
rs7792118826:146,978,013C/Tuncertain significance
rs3731184146:146,978,051G/Tuncertain significance
rs14028062286:146,987,953A/Cuncertain significance
rs11975743316:146,988,022G/Cuncertain significance
rs1409300036:146,991,069G/Aintron variant
rs7482865756:146,993,397T/Cuncertain significance
rs1908960956:146,993,450G/Auncertain significance
rs13750609456:146,993,474C/Auncertain significance
rs3742967546:146,993,477G/Auncertain significance
rs11806458616:146,993,556C/Alikely benign
rs735718706:146,993,573G/Auncertain significance
rs9447166626:146,993,601A/Guncertain significance
rs2015160356:146,997,491A/Tuncertain significance
rs7557786176:146,997,493G/Auncertain significance
rs5360439376:146,997,510C/Guncertain significance
rs5418903136:146,997,517T/Auncertain significance
rs7496788826:147,006,882T/Cuncertain significance
rs13409923876:147,006,902G/Auncertain significance
rs7760429896:147,012,387C/Tuncertain significance
rs12155707306:147,012,414G/Tuncertain significance
rs7496031576:147,014,030C/Tuncertain significance
rs10565329646:147,014,035A/Guncertain significance
rs14104022306:147,022,084G/Auncertain significance
rs7751153226:147,022,088G/Tuncertain significance
rs3774711856:147,022,091C/Tuncertain significance
rs7561574626:147,022,145C/Guncertain significance
rs9436607366:147,036,519G/Auncertain significance
rs2009965356:147,038,081G/Auncertain significance
rs13127991106:147,038,124C/Tuncertain significance
rs3705688086:147,038,138C/Tuncertain significance
rs8893319256:147,038,163A/Cuncertain significance
rs7633648726:147,038,698G/Auncertain significance
rs13297913226:147,042,581C/Guncertain significance
rs24827149136:147,045,342C/Tuncertain significance
rs1475663856:147,045,447G/Auncertain significance
rs3696356916:147,045,450C/Tuncertain significance
rs7571144476:147,045,451G/Auncertain significance
rs9844038196:147,045,454T/Guncertain significance
rs12603599486:147,047,226A/Guncertain significance
rs5696888546:147,049,720G/Auncertain significance
rs1487865476:147,054,274T/Cuncertain significance
rs10543741556:147,054,277C/Tuncertain significance
rs24827294996:147,054,290A/Tuncertain significance
rs12809647046:147,054,297A/Cuncertain significance
rs7661708716:147,054,361C/Tuncertain significance
rs24827317596:147,055,047A/Cuncertain significance
rs5699775996:147,055,052T/Cuncertain significance
rs12143794036:147,055,082G/Auncertain significance
rs8986295696:147,055,158G/Auncertain significance
rs14159378076:147,057,642G/Cuncertain significance
rs7806019896:147,057,671A/Cuncertain significance
rs7572750546:147,061,600T/Cuncertain significance
rs13389362286:147,062,361C/Guncertain significance
rs7653360906:147,062,396A/Guncertain significance
rs1422452546:147,067,206G/Auncertain significance
rs17773411546:147,073,772G/Auncertain significance
rs7711030066:147,085,064C/Guncertain significance
rs24827845926:147,085,078G/Tuncertain significance
rs24827847436:147,085,136G/Auncertain significance
rs14041906146:147,085,165G/Tuncertain significance
rs3721773756:147,085,199C/Tuncertain significance
rs2005004956:147,085,204A/Guncertain significance
rs7484341336:147,105,782A/Tuncertain significance
rs14265385446:147,105,796T/Cuncertain significance
rs5761147396:147,105,797A/Guncertain significance
rs14521066276:147,105,802A/Guncertain significance
rs3762486746:147,105,862G/Auncertain significance
rs9741090956:147,105,865A/Tuncertain significance
rs13431557646:147,106,758C/Guncertain significance
rs9077585166:147,106,768A/Tuncertain significance
rs9900609516:147,106,785A/Cuncertain significance
rs13636756946:147,106,805G/Cuncertain significance
rs7793582536:147,109,545G/Auncertain significance
rs3770511626:147,109,558A/Guncertain significance
rs3701600396:147,109,593A/Guncertain significance
rs3749601076:147,109,594T/Auncertain significance
rs7779819206:147,109,656G/Auncertain significance
rs7739356576:147,109,680G/Cuncertain significance
rs5457593406:147,109,716C/Tuncertain significance
rs24828413646:147,122,343C/Tuncertain significance
rs24828414386:147,122,388A/Guncertain significance
rs11835665656:147,122,414C/Tuncertain significance
rs7629946306:147,122,965A/Guncertain significance
rs7516891126:147,123,029C/Auncertain significance
rs10100532466:147,123,084C/Guncertain significance
rs5670952106:147,123,101G/Alikely benign
rs7797396946:147,136,176A/Tuncertain significance
rs7721700956:147,136,205T/Auncertain significance
rs11866530246:147,136,221A/Tuncertain significance
rs7758619446:147,136,238C/Tuncertain significance
rs7535117606:147,136,300A/Guncertain significance
rs13970689516:147,136,330A/Guncertain significance
rs13495083206:147,136,345A/Guncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.